ICS:11.100.10
Showing 19–27 of 41 results
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ISO 6717:2021 In vitro diagnostic medical devices – Single-use containers for the collection of specimens from humans other than blood
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ISO 18113:2022 In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 4: In vitro diagnostic reagents for self-testing
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ISO 20184:2018 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for frozen tissue – Part 2: Isolated proteins
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ISO 7552:2024 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood – Part 2: Isolated DNA
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ISO 20166:2018 Molecular in vitro diagnostic examinations – Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue – Part 2: Isolated proteins
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ISO 29701:2010 Nanotechnologies – Endotoxin test on nanomaterial samples for in vitro systems – Limulus amebocyte lysate (LAL) test
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ISO 5649:2024 Medical laboratories – Concepts and specifications for the design, development, implementation and use of laboratory-developed tests
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ISO 21151:2020 In vitro diagnostic medical devices – Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
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ISO 24443:2021/Amd 1:2026 Cosmetics — Determination of sunscreen UVA photoprotection in vitro — Amendment 1
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